Hasil Pencarian - Hafiz Muhammad Azhar Baig

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  1. 1
    P.arg102ser is a common Pde6? mutation causing autosomal recessive retinitis pigmentosa in Pakistani families

    P.arg102ser is a common Pde6? mutation causing autosomal recessive retinitis pigmentosa in Pakistani families oleh Anosha Ali Khan, Yar Muhammad Waryah, Muhammad Iqbal, Hafiz Muhammad Azhar Baig, Muhammad Rafique, Ali Muhammad Waryah

    Diterbitkan 2020-11-01
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  2. 2
    Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder

    Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder oleh Francesca Mattioli, Hossein Darvish, Sohail Aziz Paracha, Abbas Tafakhori, Saghar Ghasemi Firouzabadi, Marjan Chapi, Hafiz Muhammad Azhar Baig, Alexandre Reymond, Stylianos E. Antonarakis, Muhammad Ansar

    Diterbitkan 2021-11-01
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